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Eleven Years of Menicon Z Night Contact Lens Wear in Reducing Myopia Progression in Children

NCT04806711 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 20

Last updated 2021-03-19

No results posted yet for this study

Summary

To compare axial length growth of white European myopic children wearing Menicon Z Night orthokeratology contact lenses to a control group of distance, single-vision glasses and contact lenses over an 11-year period.

Conditions

  • Myopia, Progressive
  • Children, Only

Interventions

DEVICE

Menicon Z Night

Menicon Z Night orthokeratology contact lenses were used to assess their efficacy in reducing myopia progression in children

DEVICE

Control

Distance, single-vision glasses were used as a control

Sponsors & Collaborators

  • Universidad Europea de Madrid

    collaborator OTHER

  • Clinica novovision

    collaborator UNKNOWN

  • Menicon Co., Ltd.

    lead INDUSTRY

Study Design

Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
6 Years
Max Age
12 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2007-03-01
Primary Completion
2018-03-01
Completion
2018-03-01

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04806711 on ClinicalTrials.gov